The Opportunity
The General Manager for the Debrecen Operations will be instrumental in leading one of Teva’s largest and most strategic pivotal sites in the network. He/she will provide the leadership, direction, and overall oversight of this key site. In total, the operation has about 1,000 employees and oversees annual prod-ex of ~ 67M$, with Raw materials – all together ~ 220M$ budget management. The Site GM will be a true GM with responsibility for Production, Quality, MS&T, HR, Supply Chain, EHS, Engineering, and Finance. The Site GM will be responsible to ensure that the corporate strategy is executed efficiently and effectively. He/she will need to be an exceptional leader who can deal with a high degree of complexity and the introduction of new technologies, with strong problem solving and transformational mindset and OPEX [lean] skills.
Responsibilities
All areas of responsibility listed below are essential to the satisfactory performance of this position by any incumbents with reasonable accommodation if necessary. Any non-essential functions are assumed to be included in other related duties or assignments.
This role requires someone skilled in building a strong team culture and in developing capabilities as well as leadership skills. Specific responsibilities include:
Rebuild and reshape the employee workforce at every level.
Change the employee culture and mindset.
Support the ongoing remediation, which requires strong technical, quality and GMP leadership. A strong technical background would be a plus.
Balance short-term operational delivery and improvement needs with implementation of a longer-term strategic plan for the site – transformation ahead, need to plan long-range plan.
Support Teva’s Corporate Goals – Understand & contribute to the achievement of Teva’s goals at the regional and global levels.
Responsible for completing all training requirements and maintaining 100% compliance with all assignments.
Responsible for maintaining work areas and performing job functions in a safe and efficient manner in accordance with company policies and procedures, Good Manufacturing Practices (cGMP’s), and Standard Operating Procedures (SOP’s) instructions.
Responsible for performing additional related duties as assigned.
